Original article from Clinical Omics
There is typically much reflection whenever tipping from one decade into the next, as we look back at what has transpired over the past 10 years. When it comes to omics technologies and their application to precision medicine, there have certainly been significant advances.
Notable among them would be the completion of the 100,000 Genomes Project which both commenced and reached its final goal of 100,000 whole genomes sequenced within the decade and has served as the springboard for the launch of a genomic medicine program by England’s National Health Service. Today, there are more than a dozen country-wide efforts focused on collecting health and sequencing data of large and diverse swaths of each countries’ citizens—all with an eye toward using these vast data to improve how we provide healthcare for both large populations of patients and, ultimately, individuals.
But are we yet able to consistently provide precision medicine? In small niches, yes. So, while much progress has been made, it is fair to say more advances are needed before precision medicine and/or genomic medicine is standard practice. So how will we get there? Read on as four industry watchers share with you their thought on what may happen in the next ten years to advance the field.
Protection and Individual Control of Personal Health Data Will Fuel Research
Discovery flows from research and research requires data. This longstanding truth will dramatically change in the decade ahead through how crucial data is acquired, aggregated, controlled, and protected. This transformation will occur as a consequence of maturation in our thinking around personal data sovereignty, and accountability and transparency in data stewardship.
A marked change in public sentiment around health data privacy is afoot. Google is under investigation by the Office of Civil Rights in the Department of Health & Human Services because they partnered with Ascension, the nation’s largest nonprofit health system, which provided health data without notifying individuals that their information was disclosed. This, despite asserting that they were compliant with HIPAA regulations that protect disclosure of personal health information. And on January 1st, the strictest data privacy law in the U.S., the California Consumer Privacy Act, took effect strengthening consumer data privacy rights in the country’s most populous state.
There is a growing lack of trust among the public in the institutions holding, buying, and using people’s data, which has fueled fears that data may be used against individuals and their families—from discrimination to “tailored” information feeds. People also now better understand the value of their personal data, and that they are not sharing in the value created from it. With DNA data in particular, people are now keenly aware that this information is shared within families, as numerous 2019 headlines detailing law enforcement applications demonstrated.
Data fuels research which in turn fuels discovery, but ultimately it is people who fuel this data—sick people, healthy people, old and young people, rich and poor people, people of all colors. They are the best curators of their health condition. If the past ten years are remembered as the decade that made genome sequencing for disease research possible, I believe the next ten years will see us execute discovery with a more holistic and inclusive lens. We will broaden our study beyond disease research to human health—with ‘health’ defined as more than just the absence of disease—and quality of life with the recognition that genetics is a mere 30% contributor to premature death. Human behavioral patterns, social circumstances, health care, and environmental exposure contribute the remaining 70%. I hope transcriptomes, microbiomes, and epigenetics will complement DNA datasets, and that person-reported, real-world, and environmental information will be included.
I’ll use the next decade to champion raising the standing of people from subjects of research to partners in discovery. In our increasingly digital world, and respecting that all personal health data—including DNA, health records, social and structural determinants of health, and clinical outcomes—starts with people, it stands to reason that if people are included, it represents a step function increase in discovery. As partners in discovery, we must win people’s trust starting with transparency and assurances they are in control over how their data is used, who it’s stored with, and empower them with the ability to un-share all their data, at any time, if they wish.
Research has suffered for lack of data scale, scope, and depth, including insufficient ethnic and gender diversity, datasets that lack environment and lifestyle data, and snapshots-in-time versus longitudinal data. Artificial intelligence is starved for data that reflects population diversity and real-world information. I worry about the impact on research if people disengage with science and digital tools for fear of privacy violations. It’s time to feed discovery with data that reflects the diversity of the population we wish to serve. I believe people are the key to the next generation of discovery, and that protecting their privacy will empower discovery.
To read more from other industry watchers, click here.
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